Ivanov Alexander Vladimirovich, Virus Edward Danielevich, Nikiforova Ksenya Alexandrovna, Kushlinskii Nicolai Evgenevich, Luzyanin Boris Petrovich, Maksimova Marina Yurievna, Piradov Mikhail Aleksanrovich, Kubatiev Aslan Amirkhanovich
Federal State Budgetary Scientific Institution "Institute of General Pathology and Pathophysiology,", Moscow, Russia.
N. N. Blokhin Russian Cancer Research Center, Moscow, Russia.
Electrophoresis. 2016 Oct;37(20):2663-2669. doi: 10.1002/elps.201600242. Epub 2016 Sep 5.
An approach that allows direct analysis of the ratio of S-adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) by using CE is presented. The analytes were extracted on phenylboronic acid phase and eluted with 100 mmol/L HCl. CE separation of the analytes took place in the transient isotachophoresis mode with addition of NaCl and meglumine to the samples. The sensitivity (S/N = 3) and quantification limit (S/N = 10) of the method were 0.07 and 0.2 μmol/L, respectively, using a silica capillary with 50 μm internal diameter and 30.5 cm total length. The BGE was 0.02 mol/L Tris with 1 mol/L HCOOH (pH 2.2), and the separation voltage was 15-17 kV. Accuracy of SAM and SAH analysis in urine was 96 and 105%, respectively; interday precision for the SAM/SAH ratio was within 6%. The theoretical plate number exceeded a million. Total analysis time was 8.5 min.
提出了一种通过毛细管电泳(CE)直接分析S-腺苷甲硫氨酸(SAM)与S-腺苷高半胱氨酸(SAH)比例的方法。分析物在苯硼酸相上进行萃取,并用100 mmol/L盐酸洗脱。分析物的CE分离在加入氯化钠和葡甲胺的样品的瞬态等速电泳模式下进行。使用内径50μm、总长30.5 cm的硅胶毛细管时,该方法的灵敏度(信噪比=3)和定量限(信噪比=10)分别为0.07和0.2μmol/L。背景电解质(BGE)为含1 mol/L甲酸的0.02 mol/L Tris(pH 2.2),分离电压为15 - 17 kV。尿液中SAM和SAH分析的准确度分别为96%和105%;SAM/SAH比例的日间精密度在6%以内。理论塔板数超过一百万。总分析时间为8.5分钟。